NDC 68788-8819 – Prednisone

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8819

Product details

Brand name
Prednisone
Generic name
Prednisone
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215672
Marketed since
January 23, 2025
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Prednisone →

Package NDC codes (6)

Package NDCDescriptionSince
68788-8819-110 TABLET in 1 BOTTLE (68788-8819-1)Jan 23, 2025
68788-8819-220 TABLET in 1 BOTTLE (68788-8819-2)Jan 23, 2025
68788-8819-330 TABLET in 1 BOTTLE (68788-8819-3)Jan 23, 2025
68788-8819-418 TABLET in 1 BOTTLE (68788-8819-4)Jan 23, 2025
68788-8819-515 TABLET in 1 BOTTLE (68788-8819-5)Jan 23, 2025
68788-8819-821 TABLET in 1 BOTTLE (68788-8819-8)Jan 23, 2025

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